| Primary Device ID | 06942598201800 |
| NIH Device Record Key | 2aa1ac2b-c344-4ac9-a0ab-8cf567a4ae19 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | DrugTect Multi-Drug Urine Test Cup |
| Version Model Number | DT-AT18-FLAT-1-AZ5 |
| Company DUNS | 543254717 |
| Company Name | Hangzhou AllTest Biotech Co., Ltd. |
| Device Count | 5 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | true |
| 06942598201855 | DrugTect ,18 Panel Multi-Drug Rapid Urine Test Cup, CLIA WAIVED
(6-MAM10, AMP500, BAR300, BUP10, |
| 06942598201848 | DrugTect ,18 Panel Multi-Drug Rapid Urine Test Cup, CLIA WAIVED
(6-MAM10, AMP500, BAR300, BUP10, |
| 06942598201831 | DrugTect ,18 Panel Multi-Drug Rapid Urine Test Cup, CLIA WAIVED
(6-MAM10, AMP500, BAR300, BUP10, |
| 06942598201824 | DrugTect ,18 Panel Multi-Drug Rapid Urine Test Cup, CLIA WAIVED
(6-MAM10, AMP500, BAR300, BUP10, |
| 06942598201817 | DrugTect ,18 Panel Multi-Drug Rapid Urine Test Cup, CLIA WAIVED
(6-MAM10, AMP500, BAR300, BUP10, |
| 06942598201800 | DrugTect ,18 Panel Multi-Drug Urine Test Cup, OTC
(6-MAM10, AMP500, BAR300, BUP10,BZO300, COC150 |
| 16942598201791 | DrugTect ,18 Panel Multi-Drug Urine Test Cup, OTC
(6-MAM10, AMP500, BAR300, BUP10,BZO300, COC150 |